Waye, J S <br/><br/>
Identification of two new alpha-thalassemia mutations in exon 2 of the alpha1-globin gene.  [electronic resource] 

 -  Hemoglobin  Nov 2001 
 - 391-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0363-0269 
<br/><br/><label>Standard No.: </label>10.1081/hem-100107876  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Child<br/>Erythrocytes, Abnormal<br/>Exons<br/>Family Health<br/>Female<br/>Genetic Heterogeneity<br/>Globins--genetics<br/>Humans<br/>Male<br/>Phenotype<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Sequence Deletion<br/>alpha-Thalassemia--genetics